Evidence map›Paper›PMID 41066523›Full record

ArticlePLoS computational biology2025

Assessing parameter identifiability of a hemodynamics PDE model using spectral surrogates and dimension reduction.

Mitchel J Colebank

Abstract read
In one paragraph

Article in PLoS computational biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

1 author.

Mitchel J ColebankDepartment of Mathematics, University of South Carolina, Columbia, South Carolina, United States of America.ORCID 0000-0002-2294-9124

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Computational inverse problems for biomedical simulators suffer from limited data and relatively high parameter dimensionality. This often requires sensitivity analysis, where parameters of the model are ranked based on their influence on the specific quantities of interest. This is especially important for simulators used to build medical digital twins, as the amount of data is typically limited. For expensive models, such as blood flow models, emulation is employed to expedite the simulation time. Parameter ranking and fixing using sensitivity analysis are often heuristic, though, and vary with the specific application or simulator used. The present study provides an innovative solution to this problem by leveraging polynomial chaos expansions (PCEs) for both multioutput global sensitivity analysis and formal parameter identifiability. For the former, we use dimension reduction to efficiently quantify time-series sensitivity of a one-dimensional pulmonary hemodynamics model. We consider both Windkessel and Structured Tree boundary conditions. We then use PCEs to construct univariate profile-likelihood confidence intervals and show how changes in experimental design improve identifiability. Our work presents a novel approach to determining parameter identifiability and leverages a common emulation strategy for enabling profile-likelihood analysis in problems governed by partial differential equations.

Indexed as

HemodynamicsModels, CardiovascularAlgorithmsComputational BiologyComputer SimulationHumans

Identifiers

PMID41066523
PMCPMC12520355

What Socratic holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.